Canonical Allele Identifier: CA2675194668
Gene: MIR3936HG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132369665T>G , CM000667.2:g.132369665T>G GRCh38
NC_000005.9:g.131705357T>G , CM000667.1:g.131705357T>G GRCh37
NC_000005.8:g.131733256T>G NCBI36
NG_008982.1:g.4957T>G
NG_008982.2:g.4962T>G

Transcript Alleles

HGVS Amino-acid Change
NR_110997.1:n.73+179A>C